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Efficient One-Pot Cross-Coupling of Two Aryl Halides by Stannylation/Stille Reaction in Water under Microwave Irradiation

机译:微波辐射下水中甲锡烷基化/斯蒂尔反应的两个芳基卤化物的高效一锅交叉偶联

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摘要

A simple and highly efficient one-pot approach has been developed for the Pd(PPh3)4-catalyzed cross-coupling of two different aryl or heteroaryl bromides/iodides. This method involves the combined use of microwave irradiation and water as a single solvent to achieve sequential stannylation and Stille cross-coupling reactions, which allows rapid access to a wide variety of biaryls in good to high yields. Furthermore, utilizing this step-economical protocol, 2,5-dibromopyridine was iteratively diarylated and the Boscalid intermediate was also synthesized in a one-pot manner.
机译:对于两种不同的芳基或杂芳基溴化物/碘化物的Pd(PPh3)4催化的交叉偶联,已经开发出一种简单高效的一锅法。该方法涉及将微波辐射和水作为单一溶剂的组合使用,以实现顺序的甲锡烷基化和斯蒂勒交叉偶联反应,从而可以以高收率或高收率快速获得各种联芳基。此外,利用这种经济的步骤,将2,5-二溴吡啶重复地二芳基化,并且也以一锅法合成了Boscalid中间体。

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